GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Rhizobium etli CFN 42

Align Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.31 (characterized)
to candidate WP_020922563.1 RHE_RS20615 homoserine O-succinyltransferase

Query= SwissProt::Q7CWE8
         (308 letters)



>NCBI__GCF_000092045.1:WP_020922563.1
          Length = 307

 Score =  565 bits (1457), Expect = e-166
 Identities = 267/304 (87%), Positives = 283/304 (93%)

Query: 1   MPIKIPDTLPAFETLVHEGVRVMTETAAIRQDIRPLQIGLLNLMPNKIKTEIQMARLVGA 60
           MPIKIPDTLPAFETLV EGVRVMTET AIRQDIRPLQIGLLNLMPNKIKTE+QMARLVGA
Sbjct: 1   MPIKIPDTLPAFETLVQEGVRVMTETMAIRQDIRPLQIGLLNLMPNKIKTELQMARLVGA 60

Query: 61  SPLQVELSLIRIGGHRAKNTPEEHLLSFYQTWEEVRHRKFDGFIITGAPIELLDYEDVTY 120
           SPLQVELSLIRIGGH+AKNT E+HLL+FYQTWEEV+ RKFDGFIITGAPIELL YEDVTY
Sbjct: 61  SPLQVELSLIRIGGHKAKNTSEDHLLAFYQTWEEVKQRKFDGFIITGAPIELLPYEDVTY 120

Query: 121 WNEMQQIFEWTQTNVHSTLNVCWGAMAAIYHFHGVPKYELKEKAFGVYRHRNLSPSSIYL 180
           W EMQ+IF WT+TNVHST+NVCWGAMAAIYHFHGVPKYELKEKAFGVYRHRNL PSSIYL
Sbjct: 121 WAEMQEIFNWTETNVHSTMNVCWGAMAAIYHFHGVPKYELKEKAFGVYRHRNLKPSSIYL 180

Query: 181 NGFSDDFQVPVSRWTEVRRADIEKHPELEILMESDEMGVCLAHEKAGNRLYMFNHVEYDS 240
           NGFSD+F+VPVSRWTEVRR DIEK   LEILMES EMGVCL HEK G RLYMFNHVEYDS
Sbjct: 181 NGFSDNFEVPVSRWTEVRREDIEKSASLEILMESSEMGVCLVHEKRGRRLYMFNHVEYDS 240

Query: 241 TSLADEYFRDVNSGVPIKLPHDYFPHNDPELAPLNRWRSHAHLFFGNWINEIYQTTPYDP 300
           TSL+DEYFRDV++GVPIK+PH+YFPHNDP LAP NRWRSHAHL FGNWINEIYQTTPYD 
Sbjct: 241 TSLSDEYFRDVDAGVPIKMPHNYFPHNDPTLAPQNRWRSHAHLLFGNWINEIYQTTPYDV 300

Query: 301 QAIG 304
           + IG
Sbjct: 301 EEIG 304


Lambda     K      H
   0.321    0.137    0.429 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 462
Number of extensions: 12
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 308
Length of database: 307
Length adjustment: 27
Effective length of query: 281
Effective length of database: 280
Effective search space:    78680
Effective search space used:    78680
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory